RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET— 510(k) K130405

Name: FDA 510(k) clearance K130405
Creator: U.S. Food and Drug Administration
Published: 2013-11-06

Substantially Equivalent

Teleflex Medical

FDA 510(k) clearance K130405 for RUSCH EASYCRIC EMERGENCY CRICOTHYROTOMY SET, Substantially Equivalent on 2013-11-06. Applicant: Teleflex Medical. Device class: 2.

Clearance details

Applicant: Teleflex Medical
Product code: Code BWC
Device class: Class 2
Regulation: 21 CFR 868.5090
Advisory panel: Anesthesiology
Date received: 2013-02-19
Decision date: 2013-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Durham, NC, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.